Mapping Data Summary

• Symbol: D14Mit203
• Name: DNA segment, Chr 14, Massachusetts Institute of Technology 203
• ID: MGI:101040
• Chromosome: 14

8 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Intercross	14	J:150720 Baek IC, et al., A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis. Mamm Genome. 2009 Jun;20(6):350-8
CROSS	Cross Type: Intercross	14	J:108173 Nam Y, et al., A novel missense mutation in the mouse hairless gene causes irreversible hair loss: genetic and molecular analyses of Hr m1Enu. Genomics. 2006 Apr;87(4):520-6
TEXT		14	J:45215 McCarthy LC, et al., A first-generation whole genome-radiation hybrid map spanning the mouse genome. Genome Res. 1997 Dec;7(12):1153-61
TEXT-Genetic Cross		14	J:66648 Beamer WG, et al., Spontaneous fracture (sfx): a mouse genetic model of defective peripubertal bone formation. Bone. 2000 Nov;27(5):619-26
TEXT-Genetic Cross		14	J:112377 Mohan S, et al., Spontaneous fractures in the mouse mutant sfx are caused by deletion of the gulonolactone oxidase gene, causing vitamin C deficiency. J Bone Miner Res. 2005 Sep;20(9):1597-610
TEXT-QTL		14	J:148559 Blizard DA, et al., Blood pressure and heart rate QTL in mice of the B6/D2 lineage: sex differences and environmental influences. Physiol Genomics. 2009 Feb 2;36(3):158-66
TEXT-QTL		14	J:52903 Ewart-Toland A, et al., Effect of the genetic background on the reproduction of leptin-deficient obese mice. Endocrinology. 1999 Feb;140(2):732-8
TEXT-Radiation Hybrid		14	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;